P49104
Piperonal
99%
Synonym(s):
1,3-Benzodioxole-5-carboxaldehyde, 3,4-(Methylenedioxy)benzaldehyde, Heliotropin
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About This Item
Empirical Formula (Hill Notation):
C8H6O3
CAS Number:
Molecular Weight:
150.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-409-7
Beilstein/REAXYS Number:
131691
MDL number:
Assay:
99%
Form:
solid
InChI key
SATCULPHIDQDRE-UHFFFAOYSA-N
InChI
1S/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H2
SMILES string
[H]C(=O)c1ccc2OCOc2c1
vapor pressure
1 mmHg ( 87 °C)
assay
99%
form
solid
bp
264 °C (lit.)
mp
35-39 °C (lit.)
Quality Level
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Related Categories
signalword
Warning
hcodes
wgk
WGK 2
flash_point_f
150.1 °F
flash_point_c
65.62 °C
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Hazard Classifications
Repr. 2 - Skin Sens. 1
Storage Class
11 - Combustible Solids
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A R Dahl et al.
Biochemical pharmacology, 34(5), 631-636 (1985-03-01)
Eighteen methylenedioxyphenyl (MDP) compounds, including some commonly inhaled by people, were tested for the ability to inhibit rabbit nasal microsomal cytochrome P-450-dependent hexamethylphosphoramide (HMPA) N-demethylase. For comparison, liver microsomes were also used. Nasal cytochrome P-450 from rabbits metabolized MDP compounds
Ariel Ceferino Toloza et al.
Memorias do Instituto Oswaldo Cruz, 101(1), 55-56 (2006-05-16)
New alternative insecticides are necessary for the chemical control of head lice. In this study the fumigant knockdown time 50% (KT50) and repellency index (RI) of three aliphatic lactones was compared with two essential oils and DDVP, against permethrin-resistance Pediculus
Patricia Guerra-Diaz et al.
Analytical chemistry, 82(7), 2826-2835 (2010-03-09)
A preconcentration device that targets the volatile chemical signatures associated with illicit drugs and explosives (high and low) has been designed to fit in the inlet of an ion mobility spectrometer (IMS). This is the first reporting of a fast
The inhibition of rat nasal cytochrome P-450-dependent mono-oxygenase by the essence heliotropin (piperonal).
A R Dahl
Drug metabolism and disposition: the biological fate of chemicals, 10(5), 553-554 (1982-09-01)
J Sekizawa et al.
Mutation research, 101(2), 127-140 (1982-04-01)
The genotoxicity of safrole, 9 compounds that are structurally similar to safrole (anethole, cinnamaldehyde, cinnamyl alcohol, estragole, methyl eugenol, eugenol, isoeugenol, isosafrole, piperonal), 5 essential oils, cassia oil, cinnamon bark oil, clove oil, fennel oil) which contain the chemicals tested
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